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SCN4A as modifier gene in patients with myotonic dystrophy type 2.
Binda A, Renna LV, Bosè F, Brigonzi E, Botta A, Valaperta R, Fossati B, Rivolta I, Meola G, Cardani R. Binda A, et al. Sci Rep. 2018 Jul 23;8(1):11058. doi: 10.1038/s41598-018-29302-z. Sci Rep. 2018. PMID: 30038349 Free PMC article.
SCN4A mutation as modifying factor of myotonic dystrophy type 2 phenotype.
Bugiardini E, Rivolta I, Binda A, Soriano Caminero A, Cirillo F, Cinti A, Giovannoni R, Botta A, Cardani R, Wicklund MP, Meola G. Bugiardini E, et al. Among authors: binda a. Neuromuscul Disord. 2015 Apr;25(4):301-7. doi: 10.1016/j.nmd.2015.01.006. Epub 2015 Jan 21. Neuromuscul Disord. 2015. PMID: 25660391
Cardiac and neuronal HCN channelopathies.
Rivolta I, Binda A, Masi A, DiFrancesco JC. Rivolta I, et al. Among authors: binda a. Pflugers Arch. 2020 Jul;472(7):931-951. doi: 10.1007/s00424-020-02384-3. Epub 2020 May 18. Pflugers Arch. 2020. PMID: 32424620 Review.
Effect of the ketogenic diet in excitable tissues.
Murano C, Binda A, Palestini P, Baruscotti M, DiFrancesco JC, Rivolta I. Murano C, et al. Among authors: binda a. Am J Physiol Cell Physiol. 2021 Apr 1;320(4):C547-C553. doi: 10.1152/ajpcell.00458.2020. Epub 2021 Jan 27. Am J Physiol Cell Physiol. 2021. PMID: 33502948 Free article. Review.
Novel SCN5A p.Val1667Asp Missense Variant Segregation and Characterization in a Family with Severe Brugada Syndrome and Multiple Sudden Deaths.
Monasky MM, Micaglio E, Ciconte G, Rivolta I, Borrelli V, Ghiroldi A, D'Imperio S, Binda A, Melgari D, Benedetti S, Mitrovic P, Anastasia L, Mecarocci V, Ćalović Ž, Casari G, Pappone C. Monasky MM, et al. Among authors: binda a. Int J Mol Sci. 2021 Apr 29;22(9):4700. doi: 10.3390/ijms22094700. Int J Mol Sci. 2021. PMID: 33946750 Free PMC article.
85 results